A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589168



Internal ID21537732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48530079..48530129hg38UCSC Ensembl
chr15:48822276..48822326hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085325
SamplesHG00513
Known GenesFBN1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589168
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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